Isle Media and Sterile Products, Inc.

FDA Regulatory Profile

Isle Media and Sterile Products, Inc. appears in FDA public data with 0 recalls, 93 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 28, 1983.

Summary

Total Recalls
0
510(k) Clearances
93
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K831671MODIFIED SOYBEAN CASEIN DIGEST BROTHJuly 28, 1983
K821218CAMPY-S AGARMay 14, 1982
K820863MEDIA FOR IN-VITRO DIAGNOSTIC USEApril 16, 1982
K812798MOTILITY GI MEDIUMOctober 20, 1981
K812797SCHAEDLER AGARSOctober 20, 1981
K812795ANAEROBIC BLOOD AGAROctober 20, 1981
K812796ANAEROBIC CNA BLOOD AGAROctober 20, 1981
K800818CHLAMYDOSPORE AGARApril 24, 1980
K800807CORN MEAL AGAR MEDIAApril 24, 1980
K800333MODIFIED THAYER-MARTIN X AGARMarch 3, 1980
K800334MARTIN-LEWIS AGARMarch 3, 1980
K800156STAPHYLOCOCCUS MED. 110February 13, 1980
K800157BISMUTH SULFITE AGARFebruary 13, 1980
K800158AZIDE BLOOD AGAR BASE W/&WTHOT SHP. BLDFebruary 13, 1980
K792423TODD HEWITT BROTHJanuary 9, 1980
K792594TRYPTIC SOY AGAR W/LECITHIN & POLYSRBTE.December 31, 1979
K792422TETRATHIONATE BROTH BASEDecember 31, 1979
K792595SF MEDIUM (SF BROTH, STREPTOCOCCUSDecember 31, 1979
K792593PHENYLETHANOL AGARDecember 31, 1979
K792421DECARBOXYLASE BROTH BASE WITH OR WITH-December 31, 1979